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静脉丙种球蛋白地小鼠病毒性心肌炎T细胞亚群,NK细胞及部 …
引用本文:曾上勤,周同甫.静脉丙种球蛋白地小鼠病毒性心肌炎T细胞亚群,NK细胞及部 …[J].华西医科大学学报,1999,30(3):289-292.
作者姓名:曾上勤  周同甫
摘    要:为探讨病毒性心肌炎(VMC)免疫发病机理及静脉丙种球蛋白(IVIG)治疗VMC的作用机理,将BALB/c小鼠随机分为正常对照组、病毒模型组、IVIG保护组及IVIG治疗组,观察IVIG对小鼠脾脏T细胞亚群、NK细胞、IL-1、IL-2及外周血TNF活性的影响。结果:与正常对照组比较,病毒模型组NKC活性及CD3、CD4、CD8均明显降低,IL-1、IL-2及TNF活性明显升高,而IVIIG保护组一

关 键 词:心肌炎  丙种球蛋白  病毒性  T细胞亚群  NK细胞

Influence of intravenous-immunoglobulin on T lymphocyte subsets, NK cell and some cytokines in mice with experimental viral myocarditis]
S Zeng,T Zhou,Z He,Z Jin,M Wang,Z Wang,Y Hua,S Tang.Influence of intravenous-immunoglobulin on T lymphocyte subsets, NK cell and some cytokines in mice with experimental viral myocarditis][J].Journal of West China University of Medical Sciences,1999,30(3):289-292.
Authors:S Zeng  T Zhou  Z He  Z Jin  M Wang  Z Wang  Y Hua  S Tang
Institution:Department of Pediatrics, The Second Affiliated Hospital, WCUMS, Chengdu 610041.
Abstract:This study sought to gain an insight into the immunological pathogenesis of viral myocarditis and the mechanism of therapeutic action of intravenous-immunoglobulin (IVIG) on the disease, BALB/c mice were randomized into four groups: normal control group; "myocarditis model group", inoculated intraperitoneally with CVB3; "IVIG protection group", injected intraperitoneally with CVB3 and IVIG; and "IVIG treatment groups", injected intraperitoneally with CVB3 and IVIG. The amount of T cell in different T cell subsets and the activities of NK cell, IL-1 and IL-2 were assayed using spleen specimen while peripheral blood was used to measure TNF activity. The results showed: that in comparison with normal control, all spleen T cell subsets decreased in amount in myocarditis model group, so did its NK cell activity while its IL-1, IL-2 and TNF activities increased significantly. When compared with myocarditis model group, however, both IVIG protection group and IVIG treatment group showed significant elevation of NK cell activity and T cell subsets but reduced IL-1, IL-2 and TNF activities with no remarkable change in T cell subsets. The results of suggest that the immunological injury mediated by T cells plays a critical role in the pathogenesis of viral myocarditis. The protective and therapeutic effects of IVIG on the murine CVB3 myocarditis and the related immunological evidence of its actions may indicate the prospect that IVIG will become a potent and safe treatment for viral myocarditis in human.
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